Canonical Allele Identifier: PA645509568
Gene: MFN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439899
ClinVar RCV Id: RCV000506384 RCV000657919 RCV000789379 RCV000810445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055689.1:p.Ile513Val
CA599152
NM_014874.4:c.1537A>G